Variant report

Variant	nsv515856
Chromosome Location	chr9:116853797-116867054
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:610)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr9:116864807-116865125	K562	blood:	n/a	n/a
2	CBX3	chr9:116864794-116865133	K562	blood:	n/a	n/a
3	CBX3	chr9:116864751-116865191	HCT-116	colon:	n/a	n/a
4	CHD1	chr9:116861095-116861396	H1-hESC	embryonic stem cell:	n/a	n/a
5	CHD2	chr9:116861454-116861668	HepG2	liver:	n/a	n/a
6	CTCF	chr9:116858340-116858490	MCF-7	breast:	n/a	n/a
7	CTCF	chr9:116858360-116858510	BE2_C	brain:	n/a	n/a
8	CTCF	chr9:116860540-116860690	AG04449	skin:	n/a	n/a
9	CTCF	chr9:116858326-116858632	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr9:116858311-116858546	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr9:116858327-116858541	HepG2	liver:	n/a	n/a
12	CTCF	chr9:116858280-116858430	HRE	kidney:	n/a	n/a
13	CTCF	chr9:116858560-116858710	HVMF	connective:	n/a	n/a
14	CTCF	chr9:116861034-116861129	Pancreas_OC	pancreas:	n/a	n/a
15	CTCF	chr9:116858420-116858570	AG10803	skin:	n/a	n/a
16	CTCF	chr9:116858352-116858533	Gliobla	brain:	n/a	n/a
17	CTCF	chr9:116860980-116861130	HBMEC	blood vessel:	n/a	n/a
18	CTCF	chr9:116861020-116861170	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr9:116858380-116858534	HUVEC	blood vessel:	n/a	n/a
20	CTCF	chr9:116858380-116858530	AG09309	skin:	n/a	n/a
21	CTCF	chr9:116861020-116861170	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr9:116858200-116858490	HVMF	connective:	n/a	n/a
23	CTCF	chr9:116860980-116861130	MCF-7	breast:	n/a	n/a
24	CTCF	chr9:116858340-116858490	AG04450	lung:	n/a	n/a
25	CTCF	chr9:116861489-116861497	MCF-7	breast:	n/a	n/a
26	CTCF	chr9:116858380-116858530	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr9:116858400-116858550	GM12865	blood:	n/a	n/a
28	CTCF	chr9:116858343-116858535	MCF-7	breast:	n/a	n/a
29	CTCF	chr9:116858340-116858490	GM12869	blood:	n/a	n/a
30	CTCF	chr9:116858240-116858390	SAEC	small airway:	n/a	n/a
31	CTCF	chr9:116858360-116858510	GM12866	blood:	n/a	n/a
32	CTCF	chr9:116858387-116858498	Fibrobl	skin:	n/a	n/a
33	CTCF	chr9:116860920-116861070	BJ	skin:	n/a	n/a
34	CTCF	chr9:116858260-116858410	A549	lung:	n/a	n/a
35	CTCF	chr9:116856860-116857010	HCT-116	colon:	n/a	n/a
36	CTCF	chr9:116862348-116862410	HepG2	liver:	n/a	n/a
37	CTCF	chr9:116858335-116858561	K562	blood:	n/a	n/a
38	CTCF	chr9:116858360-116858510	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr9:116858340-116858490	HFF	foreskin:	n/a	n/a
40	CTCF	chr9:116858400-116858550	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr9:116858320-116858470	AG10803	skin:	n/a	n/a
42	CTCF	chr9:116858340-116858588	IMR90	lung:	n/a	n/a
43	CTCF	chr9:116861360-116861510	Caco-2	colon:	n/a	n/a
44	CTCF	chr9:116858360-116858510	GM12871	blood:	n/a	n/a
45	CTCF	chr9:116861004-116861118	MCF-7	breast:	n/a	n/a
46	CTCF	chr9:116858340-116858490	AG04449	skin:	n/a	n/a
47	CTCF	chr9:116858220-116858490	SK-N-SH_RA	brain:	n/a	n/a
48	CTCF	chr9:116858316-116858570	K562	blood:	n/a	n/a
49	CTCF	chr9:116861020-116861170	Caco-2	colon:	n/a	n/a
50	CTCF	chr9:116861425-116861518	H1-hESC	embryonic stem cell:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr9:116860500-116860550	HPAEpiC	pulmonary alveolar:	n/a
2	chr9:116860437-116860487	BJ	skin:	n/a
3	chr9:116860437-116860487	HMEC	breast:	n/a
4	chr9:116861404-116861454	RPTEC	kidney:	n/a
5	chr9:116859631-116859681	AG04449	skin:	fetal
6	chr9:116861442-116861492	GM19239	blood:	n/a
7	chr9:116860437-116860487	HCF	heart:	n/a
8	chr9:116860437-116860487	HRE	kidney:	n/a
9	chr9:116861288-116861338	BE2_C	brain:	n/a
10	chr9:116856710-116856760	SKMC	muscle:	n/a
11	chr9:116860500-116860550	BJ	skin:	n/a
12	chr9:116858634-116858684	HIPEpiC	eye:	n/a
13	chr9:116861532-116861582	A549	lung:	n/a
14	chr9:116858634-116858684	MCF10A-Er-Src	breast:	n/a
15	chr9:116860437-116860487	Hepatocyte	liver:	n/a
16	chr9:116858634-116858684	AG09319	gingival:	n/a
17	chr9:116860650-116860700	NHDF-neo	bronchial:	n/a
18	chr9:116861288-116861338	Hepatocyte	liver:	n/a
19	chr9:116860650-116860700	SK-N-MC	brain:	n/a
20	chr9:116856710-116856760	HL-60	blood:	n/a
21	chr9:116858634-116858684	BE2_C	brain:	n/a
22	chr9:116860650-116860700	Jurkat	blood:	n/a
23	chr9:116860437-116860487	HUVEC	blood vessel:	n/a
24	chr9:116861288-116861338	IMR90	lung:	fetal
25	chr9:116861404-116861454	AG04450	lung:	fetal
26	chr9:116856710-116856760	Hela-S3	cervix:	n/a
27	chr9:116860650-116860700	HRPEpiC	eye:	n/a
28	chr9:116861442-116861492	SAEC	small airway:	n/a
29	chr9:116861532-116861582	U87	brain:	n/a
30	chr9:116856710-116856760	AG10803	skin:	n/a
31	chr9:116858634-116858684	MCF-7	breast:	n/a
32	chr9:116861404-116861454	HCM	heart:	n/a
33	chr9:116861532-116861582	SAEC	small airway:	n/a
34	chr9:116860437-116860487	AG04450	lung:	fetal
35	chr9:116860437-116860487	HAEpiC	amniotic membrane:	n/a
36	chr9:116861288-116861338	HEEpiC	esophagus:	n/a
37	chr9:116861288-116861338	SKMC	muscle:	n/a
38	chr9:116860437-116860487	Jurkat	blood:	n/a
39	chr9:116856710-116856760	NHDF-neo	bronchial:	n/a
40	chr9:116861404-116861454	AG09309	skin:	n/a
41	chr9:116861442-116861492	LNCaP	prostate:	n/a
42	chr9:116861532-116861582	HIPEpiC	eye:	n/a
43	chr9:116861288-116861338	K562	blood:	n/a
44	chr9:116861442-116861492	K562	blood:	n/a
45	chr9:116858634-116858684	HCM	heart:	n/a
46	chr9:116858634-116858684	U87	brain:	n/a
47	chr9:116861442-116861492	PANC-1	pancreas:	n/a
48	chr9:116859631-116859681	HMEC	breast:	n/a
49	chr9:116861404-116861454	GM12892	blood:	n/a
50	chr9:116860437-116860487	PANC-1	pancreas:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr9:116856264..116859004-chr9:116870407..116871935,2	MCF-7	breast:
2	chr9:116848752..116850800-chr9:116852040..116854106,2	MCF-7	breast:
3	chr9:116845277..116847223-chr9:116852930..116854750,2	K562	blood:
4	chr9:116864243..116866474-chr9:116868618..116871598,3	MCF-7	breast:
5	chr9:116859675..116862094-chr9:116864175..116866038,2	MCF-7	breast:
6	chr9:116637031..116639708-chr9:116859646..116861440,2	MCF-7	breast:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KIF12-1	chr9:116856166-116856197	NONHSAT134365
2	lnc-KIF12-1	chr9:116855509-116855777	NONHSAT134365

No data

Variant related genes	Relation type
KIF12	TF binding region
KIF12	CpG island
ENSG00000157657	chromatin interactions
ENSG00000136883	chromatin interactions

Extended variants
information (count: 585 )
Associated
traits (count: 63 )

Variant overlapped rSNPs/rCNVs (count:585 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7854030	chr9:116853797-116853798	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75708349	chr9:116853822-116853823	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs571485567	chr9:116853834-116853835	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs537271005	chr9:116853843-116853844	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs79261372	chr9:116853857-116853858	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs377137447	chr9:116853862-116853863	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541704729	chr9:116853870-116853871	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535961610	chr9:116853876-116853877	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs117284126	chr9:116853907-116853908	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs572716669	chr9:116853914-116853915	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs181056885	chr9:116853946-116853947	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558850223	chr9:116853969-116853970	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369472163	chr9:116854113-116854114	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs372948199	chr9:116854123-116854124	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs201940729	chr9:116854131-116854132	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs377736009	chr9:116854133-116854134	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs143019526	chr9:116854145-116854146	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs530640960	chr9:116854149-116854150	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs371412257	chr9:116854172-116854173	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs150514063	chr9:116854175-116854176	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs116937342	chr9:116854176-116854177	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs117751044	chr9:116854183-116854184	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
23	rs200697165	chr9:116854202-116854203	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
24	rs145530814	chr9:116854209-116854210	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
25	rs374850339	chr9:116854211-116854212	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
26	rs370128201	chr9:116854212-116854213	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
27	rs367792905	chr9:116854222-116854223	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
28	rs560548665	chr9:116854227-116854228	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
29	rs370618777	chr9:116854272-116854273	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
30	rs372047743	chr9:116854278-116854279	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
31	rs552581304	chr9:116854298-116854299	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
32	rs565211937	chr9:116854299-116854300	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
33	rs376876213	chr9:116854320-116854321	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
34	rs530816861	chr9:116854348-116854349	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
35	rs41277735	chr9:116854361-116854362	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs112836320	chr9:116854373-116854374	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
37	rs546352305	chr9:116854376-116854377	Strong transcription Weak transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
38	rs566541433	chr9:116854444-116854445	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538283885	chr9:116854513-116854514	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs114068001	chr9:116854542-116854543	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs575580772	chr9:116854587-116854588	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs538105323	chr9:116854598-116854599	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555152437	chr9:116854604-116854605	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs201532959	chr9:116854628-116854629	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541326702	chr9:116854640-116854641	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs71503587	chr9:116854666-116854667	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs200839093	chr9:116854684-116854685	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs200181649	chr9:116854689-116854690	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs147277754	chr9:116854714-116854715	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs368253429	chr9:116854718-116854719	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:63)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
Renal cell carcinoma	18592004	CNVD
Developmental delay	19490664	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pleomorphic xanthoastrocytoma	20730472	CNVD
Medulloblastoma	21979893	CNVD
microdeletion syndrome	16199537	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Renal cell carcinoma	21668985	CNVD
Autism	22495311	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Myelofibrosis	22110671	CNVD
lymphocytic leukemia	21291569	CNVD
Leukemia	17361228	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Glioblastoma	16823260	CNVD
Non-small cell lung cancer	21044232	CNVD
Brain cancer	20823417	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Astrocytoma	17387387	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Renal cell carcinoma	19461508	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Heart disease	21282601	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Gastric cancer	17908304	CNVD
small cell lung cancer	20016488	CNVD
Cardiac fibroma	18329553	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	21364760	CNVD
Developmental delay	21147756	CNVD
Lung cancer	19147751	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16272173	CNVD
Bladder cancer	21909424	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21509527	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cervical cancer	16585170	CNVD
Ependymoma	19289631	CNVD
Melanoma	17363583	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:410 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:116843000-116858800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr9:116844800-116855400	Weak transcription	Gastric	stomach
3	chr9:116845200-116854200	Weak transcription	Pancreas	Pancrea
4	chr9:116845200-116854600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr9:116845200-116855000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr9:116846200-116854400	Weak transcription	Liver	Liver
7	chr9:116847400-116856400	Weak transcription	Fetal Kidney	kidney
8	chr9:116849000-116858800	Weak transcription	HepG2	liver
9	chr9:116850600-116856800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr9:116851200-116857400	Strong transcription	Fetal Intestine Small	intestine
11	chr9:116853000-116854000	Weak transcription	Fetal Stomach	stomach
12	chr9:116853000-116858600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr9:116853200-116858400	Strong transcription	Fetal Intestine Large	intestine
14	chr9:116854000-116854400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
15	chr9:116854000-116857200	Strong transcription	Fetal Stomach	stomach
16	chr9:116854000-116858600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr9:116854200-116854400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr9:116854200-116858600	Strong transcription	Pancreas	Pancrea
19	chr9:116854400-116857000	Weak transcription	Rectal Mucosa Donor 29	rectum
20	chr9:116854400-116858200	Strong transcription	Liver	Liver
21	chr9:116854600-116857000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr9:116854800-116859600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr9:116855000-116858400	Strong transcription	Duodenum Mucosa	Duodenum
24	chr9:116855000-116858800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr9:116855400-116855800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr9:116855400-116858800	Strong transcription	Gastric	stomach
27	chr9:116855400-116859800	Weak transcription	Lung	lung
28	chr9:116855400-116859800	Weak transcription	Rectal Mucosa Donor 31	rectum
29	chr9:116855600-116855800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
30	chr9:116855800-116858600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr9:116856400-116858000	Strong transcription	Fetal Kidney	kidney
32	chr9:116856400-116859800	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr9:116857000-116857400	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr9:116857000-116859200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr9:116857200-116857400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
36	chr9:116857200-116857400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
37	chr9:116857400-116858400	Genic enhancers	Fetal Intestine Small	intestine
38	chr9:116857400-116859800	Weak transcription	Rectal Mucosa Donor 29	rectum
39	chr9:116857600-116857800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr9:116857800-116858000	Bivalent/Poised TSS	Primary neutrophils fromperipheralblood	blood
41	chr9:116858000-116858200	Genic enhancers	Fetal Kidney	kidney
42	chr9:116858000-116858400	Weak transcription	Stomach Mucosa	stomach
43	chr9:116858200-116859400	Weak transcription	Fetal Kidney	kidney
44	chr9:116858200-116859800	Weak transcription	Liver	Liver
45	chr9:116858400-116859000	Genic enhancers	Fetal Intestine Large	intestine
46	chr9:116858400-116859400	Weak transcription	Duodenum Mucosa	Duodenum
47	chr9:116858400-116860000	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
48	chr9:116858600-116859000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr9:116858600-116859600	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr9:116858600-116859600	Genic enhancers	Pancreas	Pancrea

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links